A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436758



Internal ID21094311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114853813..114860768hg38UCSC Ensembl
chr10:116613572..116620527hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg386956
hg196956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197069
Samples
Known GenesFAM160B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436758
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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